ENST00000281928.9:c.5593C>T
MANE Select
|
ENSP00000281928.3:p.Arg1865Trp
|
|
ENST00000548694.2:n.583C>T
|
|
|
ENST00000648379.1:n.3961C>T
|
|
|
ENST00000648737.1:n.5357C>T
|
|
|
ENST00000648825.1:n.3778C>T
|
|
|
ENST00000648916.1:n.3604C>T
|
|
|
ENST00000649607.1:c.3777C>T
|
|
|
ENST00000649775.1:c.2082C>T
|
|
|
ENST00000650226.1:c.5629C>T
|
ENSP00000496981.1:p.Arg1877Trp
|
|
ENST00000281928.7:c.5593C>T
|
ENSP00000281928.3:p.Arg1865Trp
|
|
ENST00000548694.1:n.583C>T
|
|
|
ENST00000552447.1:c.206C>T
|
|
|
NM_015335.4:c.5593C>T
|
NP_056150.1:p.Arg1865Trp
|
|
XM_011538080.1:c.5629C>T
|
XP_011536382.1:p.Arg1877Trp
|
|
XM_011538081.1:c.5626C>T
|
XP_011536383.1:p.Arg1876Trp
|
|
XM_011538082.1:c.5599C>T
|
XP_011536384.1:p.Arg1867Trp
|
|
XM_011538080.2:c.5629C>T
|
XP_011536382.1:p.Arg1877Trp
|
|
XM_011538081.2:c.5626C>T
|
XP_011536383.1:p.Arg1876Trp
|
|
XM_011538082.2:c.5599C>T
|
XP_011536384.1:p.Arg1867Trp
|
|
XM_017019090.1:c.5590C>T
|
XP_016874579.1:p.Arg1864Trp
|
|
NM_015335.5:c.5593C>T
MANE Select
|
NP_056150.1:p.Arg1865Trp
|
|